Canonical Allele Identifier: CA474802988

Gene: SDHAF2

Linked Data

• ClinVar Variation Id: 1135179
• ClinVar RCV Id: RCV001470363
• dbSNP Id: rs2134892495
• MyVariant Identifiers: chr11:g.61205294A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437822A>G , CM000673.2:g.61437822A>G	GRCh38
NC_000011.9:g.61205294A>G , CM000673.1:g.61205294A>G	GRCh37
NC_000011.8:g.60961870A>G	NCBI36
NG_023393.1:g.12698A>G , LRG_519:g.12698A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.234A>G MANE Select	ENSP00000301761.3:p.Gly78=
ENST00000301761.6:c.234A>G	ENSP00000301761.2:p.Gly78=
ENST00000359614.9:c.234A>G	ENSP00000352630.5:p.Gly78=
ENST00000534878.5:c.234A>G	ENSP00000471030.1:p.Gly78=
ENST00000536250.1:c.*236A>G	ENSP00000471120.1:n.*236A>G
ENST00000536670.5:n.260A>G
ENST00000537782.5:c.234A>G	ENSP00000469951.1:p.Gly78=
ENST00000538594.5:c.234A>G	ENSP00000440939.1:p.Gly78=
ENST00000541135.5:c.234A>G	ENSP00000443130.1:p.Gly78=
ENST00000542074.1:c.36+7640A>G	ENSP00000469670.1:n.36+7640A>G
ENST00000542794.5:c.*236A>G	ENSP00000439983.1:n.*236A>G
ENST00000543044.2:c.198A>G	ENSP00000440219.1:p.Gly66=
ENST00000543265.1:c.234A>G	ENSP00000443660.1:p.Gly78=
ENST00000544025.5:n.329A>G
ENST00000544801.5:c.234A>G	ENSP00000442581.1:p.Gly78=
ENST00000544880.1:n.238A>G
NM_017841.2:c.234A>G , LRG_519t1:c.234A>G	NP_060311.1:p.Gly78=
NM_017841.4:c.234A>G MANE Select	NP_060311.1:p.Gly78=